Variant #0000556864 (NC_000016.9:g.15870032A>G, NM_001040113.1:c.813T>C (MYH11))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15870032A>G
DNA change (hg38) g.15776175A>G
Published as MYH11(NM_001040113.2):c.813T>C (p.Y271=), MYH11(NM_002474.3):c.792T>C (p.(Tyr264=))
ISCN -
DB-ID MYH11_000115 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0292 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 -?/. - c.813T>C r.(?) p.(Tyr271=)
MYH11 NM_002474.2 -?/. - c.792T>C r.(?) p.(Tyr264=)
NDE1 NM_017668.2 -?/. - c.*51924A>G r.(=) p.(=)


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